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Items: 1 to 20 of 94

1.

Genome-wide association mapping of QTLs implied in potato virus Y population sizes in pepper: evidence for widespread resistance QTL pyramiding.

Tamisier L, Szadkowski M, Nemouchi G, Lefebvre V, Szadkowski E, Duboscq R, Santoni S, Sarah G, Sauvage C, Palloix A, Moury B.

Mol Plant Pathol. 2019 Oct 11. doi: 10.1111/mpp.12874. [Epub ahead of print]

PMID:
31605444
2.

Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.

Zawerton A, Mignot C, Sigafoos A, Blackburn PR, Haseeb A, McWalter K, Ichikawa S, Nava C, Keren B, Charles P, Marey I, Tabet AC, Levy J, Perrin L, Hartmann A, Lesca G, Schluth-Bolard C, Monin P, Dupuis-Girod S, Guillen Sacoto MJ, Schnur RE, Zhu Z, Poisson A, El Chehadeh S, Alembik Y, Bruel AL, Lehalle D, Nambot S, Moutton S, Odent S, Jaillard S, Dubourg C, Hilhorst-Hofstee Y, Barbaro-Dieber T, Ortega L, Bhoj EJ, Masser-Frye D, Bird LM, Lindstrom K, Ramsey KM, Narayanan V, Fassi E, Willing M, Cole T, Salter CG, Akilapa R, Vandersteen A, Canham N, Rump P, Gerkes EH, Klein Wassink-Ruiter JS, Bijlsma E, Hoffer MJV, Vargas M, Wojcik A, Cherik F, Francannet C, Rosenfeld JA, Machol K, Scott DA, Bacino CA, Wang X, Clark GD, Bertoli M, Zwolinski S, Thomas RH, Akay E, Chang RC, Bressi R, Sanchez Russo R, Srour M, Russell L, Goyette AE, Dupuis L, Mendoza-Londono R, Karimov C, Joseph M, Nizon M, Cogné B, Kuechler A, Piton A; Deciphering Developmental Disorder Study, Klee EW, Lefebvre V, Clark KJ, Depienne C.

Genet Med. 2019 Oct 3. doi: 10.1038/s41436-019-0657-0. [Epub ahead of print]

PMID:
31578471
3.

SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair.

Miao Q, Hill MC, Chen F, Mo Q, Ku AT, Ramos C, Sock E, Lefebvre V, Nguyen H.

Nat Commun. 2019 Sep 6;10(1):4042. doi: 10.1038/s41467-019-11880-9.

4.

SOX9 in cartilage development and disease.

Lefebvre V, Angelozzi M, Haseeb A.

Curr Opin Cell Biol. 2019 Aug 1;61:39-47. doi: 10.1016/j.ceb.2019.07.008. [Epub ahead of print] Review.

PMID:
31382142
5.

SOXopathies: Growing Family of Developmental Disorders Due to SOX Mutations.

Angelozzi M, Lefebvre V.

Trends Genet. 2019 Sep;35(9):658-671. doi: 10.1016/j.tig.2019.06.003. Epub 2019 Jul 6. Review.

PMID:
31288943
6.

The SOXE transcription factors-SOX8, SOX9 and SOX10-share a bi-partite transactivation mechanism.

Haseeb A, Lefebvre V.

Nucleic Acids Res. 2019 Jul 26;47(13):6917-6931. doi: 10.1093/nar/gkz523.

7.

De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

Zawerton A, Yao B, Yeager JP, Pippucci T, Haseeb A, Smith JD, Wischmann L, Kühl SJ, Dean JCS, Pilz DT, Holder SE; Deciphering Developmental Disorders Study; University of Washington Center for Mendelian Genomics, McNeill A, Graziano C, Lefebvre V.

Am J Hum Genet. 2019 Apr 4;104(4):777. doi: 10.1016/j.ajhg.2019.01.014. No abstract available.

8.

Roles and regulation of SOX transcription factors in skeletogenesis.

Lefebvre V.

Curr Top Dev Biol. 2019;133:171-193. doi: 10.1016/bs.ctdb.2019.01.007. Epub 2019 Feb 26.

PMID:
30902252
9.

De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

Zawerton A, Yao B, Yeager JP, Pippucci T, Haseeb A, Smith JD, Wischmann L, Kühl SJ, Dean JCS, Pilz DT, Holder SE; Deciphering Developmental Disorders Study; University of Washington Center for Mendelian Genomics, McNeill A, Graziano C, Lefebvre V.

Am J Hum Genet. 2019 Feb 7;104(2):246-259. doi: 10.1016/j.ajhg.2018.12.014. Epub 2019 Jan 17. Erratum in: Am J Hum Genet. 2019 Apr 4;104(4):777.

10.

Sox12 promotes T reg differentiation in the periphery during colitis.

Tanaka S, Suto A, Iwamoto T, Kageyama T, Tamachi T, Takatori H, Suzuki K, Hirose K, Ohara O, Lefebvre V, Nakajima H.

J Exp Med. 2018 Oct 1;215(10):2509-2519. doi: 10.1084/jem.20172082. Epub 2018 Sep 6.

11.

SOX9 is dispensable for the initiation of epigenetic remodeling and the activation of marker genes at the onset of chondrogenesis.

Liu CF, Angelozzi M, Haseeb A, Lefebvre V.

Development. 2018 Jul 18;145(14). pii: dev164459. doi: 10.1242/dev.164459.

12.

Cancer-predicting transcriptomic and epigenetic signatures revealed for ulcerative colitis in patient-derived epithelial organoids.

Sarvestani SK, Signs SA, Lefebvre V, Mack S, Ni Y, Morton A, Chan ER, Li X, Fox P, Ting A, Kalady MF, Cruise M, Ashburn J, Stiene J, Lai W, Liska D, Xiang S, Huang EH.

Oncotarget. 2018 Jun 19;9(47):28717-28730. doi: 10.18632/oncotarget.25617. eCollection 2018 Jun 19.

13.

Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).

Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, Feitz WF, van Eerde AM, Lefebvre V, Knoers NVAM, Tabatabaei M, Schulz H, McNeill H, Schaefer F, Wegner M, Sock E, Schedl A.

Kidney Int. 2018 May;93(5):1142-1153. doi: 10.1016/j.kint.2017.11.026. Epub 2018 Feb 17.

14.

PRC2 Is Dispensable in Vivo for β-Catenin-Mediated Repression of Chondrogenesis in the Mouse Embryonic Cranial Mesenchyme.

Ferguson J, Devarajan M, DiNuoscio G, Saiakhova A, Liu CF, Lefebvre V, Scacheri PC, Atit RP.

G3 (Bethesda). 2018 Feb 2;8(2):491-503. doi: 10.1534/g3.117.300311.

15.

Inflammatory Cytokines Stabilize SOXC Transcription Factors to Mediate the Transformation of Fibroblast-Like Synoviocytes in Arthritic Disease.

Bhattaram P, Muschler G, Wixler V, Lefebvre V.

Arthritis Rheumatol. 2018 Mar;70(3):371-382. doi: 10.1002/art.40386. Epub 2018 Feb 6.

16.

SOX5/6/21 Prevent Oncogene-Driven Transformation of Brain Stem Cells.

Kurtsdotter I, Topcic D, Karlén A, Singla B, Hagey DW, Bergsland M, Siesjö P, Nistér M, Carlson JW, Lefebvre V, Persson O, Holmberg J, Muhr J.

Cancer Res. 2017 Sep 15;77(18):4985-4997. doi: 10.1158/0008-5472.CAN-17-0704. Epub 2017 Jul 7.

17.

SoxC Transcription Factors Promote Contralateral Retinal Ganglion Cell Differentiation and Axon Guidance in the Mouse Visual System.

Kuwajima T, Soares CA, Sitko AA, Lefebvre V, Mason C.

Neuron. 2017 Mar 8;93(5):1110-1125.e5. doi: 10.1016/j.neuron.2017.01.029. Epub 2017 Feb 16.

18.

Editorial for the special issue on Cartilage Biology and Pathology.

Lefebvre V.

Semin Cell Dev Biol. 2017 Feb;62:1-2. doi: 10.1016/j.semcdb.2017.01.008. No abstract available.

PMID:
28215523
19.

Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice.

Zhang H, Kamiya N, Tsuji T, Takeda H, Scott G, Rajderkar S, Ray MK, Mochida Y, Allen B, Lefebvre V, Hung IH, Ornitz DM, Kunieda T, Mishina Y.

PLoS Genet. 2016 Dec 27;12(12):e1006510. doi: 10.1371/journal.pgen.1006510. eCollection 2016 Dec.

20.

Transcriptional control of chondrocyte specification and differentiation.

Liu CF, Samsa WE, Zhou G, Lefebvre V.

Semin Cell Dev Biol. 2017 Feb;62:34-49. doi: 10.1016/j.semcdb.2016.10.004. Epub 2016 Oct 19. Review.

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